Canonical Allele Identifier: PA2826567071
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 439319

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Leu167Ser
CA397840264
NM_001276761.3:c.500T>C